Class II — Corin Ltd
| Recalling firm | Corin Group |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging. |
| Product | Unity Total Knee System. Used for knee prosthesis in total knee replacement |
| Quantity | 4 devices |
| Distribution | Distribution in the US to New Jersy and Puerto Rico. International distribution to South Africa and France. |
| Initiated | 2022-10-31 |
| Classified | 2022-11-21 |
| Terminated | 2024-01-12 |
| Recall number | Z-0273-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Corin Ltd (Z-0273-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91039/
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